CAS: 654-42-2; 2,6-Dimethylhydroquinone

该化合物是一种替代的氢解分泌衍生物,在芳香环的2和6个位置上有两个甲基组,该化合物是有机合成的多用途中间体,特别是在抗氧化剂,药物和特殊聚合物的生产方面,其苯球结构在极大程度上阻碍着稳定性,使其在需要抗氧化的用途方面有所帮助.复合物显示有机溶剂具有有利的溶解性,有助于将其纳入各种反应系统.此外,其电子刺激的甲基组影响反应性,能够选择性地实现功能化. 2,6-二甲基氢丙酮因其在控制性反应性和稳定性至关重要的高度合成高性能材料和精细化学品方面所发挥的作用而受到重视.

结构式图片

欧盟法规

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上下游产品

CAS号527-61-7 2,6-二甲基对苯醌 | CAS号576-26-1 2,6-二甲基苯酚 | CAS号2233-18-3 3,5-二甲基-4-羟基苯甲醛 | CAS号67-56-1 甲醇 | CAS号123-31-9 对苯二酚 | CAS号750624-36-3 1,3-dimethyl-2,... | CAS号187873-55-8 2,6-dimethylcyc... | CAS号78877-83-5 4-(cyclopenten-... | CAS号78877-81-3 4-(cyclopenten-... | CAS号2431-91-6 Phenol,4-methox... | CAS号527-61-7 2,6-二甲基对苯醌 | CAS号30771-74-5 2-(benzenesulfo... | CAS号4906-22-3 3,3'5,5'-四甲基-4,... | CAS号22460-32-8 1-(bromomethyl)... | CAS号21111-81-9 1,4-Benzenediol... | CAS号15770-88-4 1,4-Benzenediol... | CAS号15967-53-0 1,3-bis(chlorom... | CAS号31404-85-0 Benzaldehyde,3,... | CAS号2431-91-6 Phenol,4-methox... | CAS号708-31-6 4-羟基-2,6-二甲基苯甲酸甲酯

合成工艺路线路线简述

  • 合成目标产物 2,6-Dimethylhydroquinone 主要起始原料 2,6-Dimethylphenol
  • (文献来源)合成步骤主要原料 2,6-Dimethylphenol
2,6-二甲基-2,5-环己二烯-1,4-二酮置于三乙胺体系中,用 乙腈 作为反应溶剂,化学反应生成 2,6-二甲基-1,4-苯二酚
参考文献:对苯醌的光还原:醇和胺对溶液中中间体和反应性的影响¶
标题:对苯醌的光还原:醇和胺对溶液中中间体和反应性的影响¶
摘要:摘要 1,4-苯醌 (Bq) 和烷基-,Cl-和相关衍生物的光化学,例如甲基-,2,6-二甲基-,氯-,2,5-二氯-1,4-苯醌,Duroquinone 和使用 308 Nm 纳秒激光脉冲通过紫外-可见光谱在非水溶剂中研究了氯苯醌.在没有水的情况下,醌与 2-丙醇的三重态 (3Q*) 的反应性对于 Bq 最大,主要取决于醌结构,而来自胺的电子转移速率常数,例如三乙胺 (Tea)或 1,4-二氮杂双环 [2.2.2] 辛烷,接近 Bq 和大多数衍生物的扩散控制极限.时间分辨电导率测量支持电子从胺转移到 3Q* 后的光致电荷分离以及随后的电荷重组或中和.半醌自由基 (•qh/q•-) 衰变动力学的半衰期在很大程度上取决于供体和介质.在各种条件下测量到对苯二酚的光转化,量子产率 λirr = 254 Nm,随着 2-丙醇和 Tea 浓度的增加而增加.概述了 3Q*,•qh/q•-自由基和光
DOI:10.1562/0031-8655(2003)078<0440:Popeoa>2.0.Co;2

海关参考信息

专利信息


专利号:US-3663578-A
优先权日:1969-10-18
标题 :Catalytic oxidation of alkyl-substituted hydroquinones to the corresponding p-benzoquinones
发明人:KUTEPOW NIKOLAUS VON; MAGIN AUGUST; JOSCHEK HANS-INGO
权利人:BASF AG
摘要:AIR OXIDATION OF ALKYL-SUBSTITUTED HYDROQUINONES IN THE PRESENCE OF HEAVY METAL SALTS AS CATALYSTS IN A LIQUID MIXED PHASE CONSISTING OF AN AQUEOUS PHASE AND AN ORGANIC PHASE. THE AQUEOUS PHASE CONTAINS DISSOLVED CATALYST AND ADDITIVES FOR SETTING UP A PH BELOW 7, AND THE ORGANIC PHASE IS A SELECTIVE SOLVENT FOR THE ALKYL-SUBSTITUTED PBENZOQUINONE FORMED IN THE OXIDATION. THE PROCESS ENABLES 2,3,6-TRIMETHYLHYDROQUINONE, AN IMPORTANT INTERMEDIATE IN THE SYNTHESIS OF VITMIN E, TO BE SEPARATED FROM MIXTURES OF METHYL-SUBSTITUTED HYDROQUINONES.

专利号:US-2002185368-A1
优先权日:2001-06-07
标题:Synthesis of organic nanotubes and synthesis of ultrathin nanowires using same as templates

专利号:US-6762331-B2
优先权日:2001-06-07
标 题:Synthesis of organic nanotubes and synthesis of ultrathin nanowires using same as templates
发明人:HONG BYUNG HEE; LEE CHI-WAN; KIM KWANG SOO
权利人:POSTECH FOUNDATION
摘要:The present invention discloses a method for synthesizing a calix[4]hydroquinone organic nanotube and a method for synthesizing an ultrathin, stable nanowire using said organic nanotube as a template.

专利号:EP-1756190-B1
优先权日:2004-04-14
标 题:Radically curable resin compositions
发明人:JANSEN JOHAN FRANZ GRADUS ANTO; DRIESSEN MARCO MARCUS MATHEUS; VAN DIJCK MICHAEL ALPHONSUS CO
权利人:DSM IP ASSETS BV
摘要:The present invention relates to resin compositions for radical curing comprising a component (I) containing reactive carbon-carbon unsaturations and a component (II) containing XH-groups, with X not being C or O., which resin compositions (a) are substantially free of photoinitiators; (b.) have an average number of reactive carbon-carbon unsaturations of component (I) equal to or higher than 2; (c) have an average number of XH-groups of component (II) equal to or higher than 2; (d) whereby at least one of the average numbers of (b) and (c) is higher than 2; (e) and at most 5 mol% of the reactive unsaturations is capable of undergoing homopolymerisation; (f) respectively is present in the form of a mono-ene functional alkylene; and (g) the molar ratio of the XH-groups and of the reactive unsaturations is in the range of from 4 : 1 to 1 : 4. < >The present invention also relates to processes for curing such resin compositions, in particular by cold curing. And finally, the present invention also relates to a new process for the synthesis of Diels-Alder adducts of cyclopentadiene and a resin component containing telechelic carbon-carbon unsaturation. < >The resin compositions are capable of providing constructive materials with tack-free surfaces by fast, and tunable, radical curing, and without any problems of so-called oxygen inhibition. Suitable applications are in chemical anchoring, roofing, flooring, (re)-lining, SMCs and BMCs.

专利号:US-10407676-B2
优先权日:2014-12-09
标题 :High efficiency, small volume nucleic acid synthesis
发明人:POEHMERER THOMAS; KUHN PHILLIP; NOTKA FRANK; ZEIDLER ANDREAS; HEIL KORBINIAN; TREFZER AXEL; FONNUM GEIR; KATZEN FEDERICO; ANDERSSON KRISTIAN
权利人:LIFE TECHNOLOGIES CORP; THERMO FISHER SCIENT GENEART GMBH; LIFE TECH AS
摘要:The disclosure generally relates to compositions and methods for the production of nucleic acid molecules. In some aspects, the invention allows for the microscale generation of nucleic acid molecules, optionally followed by assembly of these nucleic acid molecules into larger molecules. In some aspects, the invention allows for efficient production of nucleic acid molecules (e.g., large nucleic acid molecules such as genomes).

专利号:EP-3837247-B1
优先权日:2018-08-17
标 题 :Synthesis of chromanol derivatives
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主要参考文献

参考标题:Synthesis Of Vitamin E Analogues: Possible Active Forms Of Vitamin E
作者:Toshie Fujishima,Hiroyuki Kagechika,Koichi Shudo
摘要:We Synthesized Several Vitamin E Analogues Containing Oxygenated Functional Groups In Place Of The 8‐methyl Group Which Is Common To All The Natural Vitamin E Congeners, Based On The Hypothesis That The Methyl Group Might Be Metabolically Oxidized To Produce Active Forms Which Might Have Specific Functions Other Than The Antioxidant Function. All The Vitamin E Analogues Examined Had Antioxidant Activity

合成参考文献


摘要:Indian Journal of Experimental Biology., 2(23), 1964
摘要:Balci, M.; Gültekin, M. S.; Çelik, M., Science of Synthesis, (2006) 28, 170.
摘要:Marsini, M. A.; Pettus, T. R. R., Science of Synthesis, (2007) 31, 450.
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